Medical Therapy for Pulmonary Arterial Hypertension*

Transcription

CHEST
Clinical Practice Guidelines
Medical Therapy for Pulmonary Arterial
Hypertension*
Updated ACCP Evidence-Based Clinical Practice
Guidelines
David B. Badesch, MD, FCCP; Steven H. Abman, MD; Gerald Simonneau, MD;
Lewis J. Rubin, MD, FCCP; and Vallerie V. McLaughlin, MD, FCCP
A consensus panel convened by the American College of Chest Physicians developed guidelines
for the treatment of pulmonary arterial hypertension (PAH) that were published in 2004.
Subsequently, several important clinical trials have been published, and new treatments have
received regulatory approval. In addition, add-on and combination therapy are being explored,
which promise to open new therapeutic avenues. This article, taking into consideration studies
published prior to September 1, 2006, provides an update to the previously published guidelines.
The original guidelines have been summarized, a discussion of new studies has been added, and
the treatment algorithm has been revised to take into account recent developments in therapy.
This update provides evidence-based treatment recommendations for physicians involved in the
care of patients with PAH. Due to the complexity of the diagnostic evaluation required and the
treatment options available, referral of patients with PAH to a specialized center continues to be
strongly recommended.
(CHEST 2007; 131:1917–1928)
Key words: anticoagulation; arginine; beraprost; bosentan; calcium-channel blockers; endothelin; endothelin receptor
antagonist; epoprostenol; idiopathic pulmonary arterial hypertension; iloprost; medical therapy; oxygen; primary
pulmonary hypertension; prostacyclin; pulmonary arterial hypertension; pulmonary hypertension; secondary pulmonary
hypertension; sildenafil; therapy; treatment; treprostinil; vasoreactivity; warfarin
Abbreviations: ACCP ⫽ American College of Chest Physicians; CCB ⫽ calcium-channel blockers; FDA ⫽ Food and
Drug Administration; IPAH ⫽ idiopathic pulmonary arterial hypertension; 6MW ⫽ 6-min walk; NYHA ⫽ New York
Heart Association; PAH ⫽ pulmonary arterial hypertension; PAPm ⫽ mean pulmonary arterial pressure;
PH ⫽ pulmonary hypertension; PVR ⫽ pulmonary vascular resistance; RCT ⫽ randomized clinical trial
arterial hypertension (PAH), defined
P asulmonary
a mean pulmonary artery pressure (PAPm)
ⱖ 25 mm Hg with a pulmonary capillary wedge
pressure ⱕ 15 mm Hg measured by cardiac catheterization, is a disorder that may occur either in the
setting of a variety of underlying medical conditions
or as a disease that uniquely affects the pulmonary
circulation. Irrespective of its etiology, PAH is a
serious and often progressive disorder that results in
right ventricular dysfunction and impairment in activity tolerance, and may lead to right-heart failure
and death. The pathogenesis of PAH is complex and
incompletely understood, but includes both genetic
and environmental factors that alter vascular structure and function.
Dramatic advances in the treatment of PAH have
occurred over the past 2 decades, based in part on
seminal observations on pathogenesis made in the
www.chestjournal.org
Downloaded From: http://journal.publications.chestnet.org/ on 09/09/2014
research laboratory. Recognizing the need to educate physicians on the diagnosis and management of
PAH, the American College of Chest Physicians
(ACCP) convened a multidisciplinary panel of experts from 2003 to 2004 to formulate guidelines for
the approach to management of this complex condition. These evidence-based guidelines, including a
comprehensive overview of treatment,1 were published as a supplement to CHEST in 2004.1– 8 The
guidelines from this original publication are presented in Table 1.
The pace of developments in the treatment for
PAH has quickened, with several important clinical
trials having been published over the past 2 years
that have led to regulatory approval of newer drugs
and experience with combinations of existing drugs.
These advances are likely to impact on the way
physicians should now approach the treatment of
CHEST / 131 / 6 / JUNE, 2007
1917
PAH. Accordingly, the ACCP impaneled a subcommittee of the original panel to develop an update to
the treatment guidelines based on these recent
developments. As before, these guidelines are evidence based and the subcommittee employed the
same criteria for inclusion and recommendation as
were used in the previous work.
Update of Treatment Guidelines
A consensus panel convened by the ACCP developed guidelines for the diagnosis and treatment of
PAH that were published in 2004.9 Subsequently,
several important clinical trials have been published
and new treatments have received regulatory approval. In addition, add-on and combination therapy
are being explored, which promise to open new
therapeutic avenues.
Therefore, the Health and Science Policy Com*From the University of Colorado Health Sciences Center (Dr.
Badesch), Denver, CO; The Children’s Hospital (Dr. Abman),
Denver, CO; Hoˆpital Antoine Be´cle`re (Dr. Simonneau), Clamart,
France; University of California, San Diego (Dr. Rubin), San
Diego, CA; and University of Michigan (Dr. McLaughlin), Ann
Arbor, MI.
Dr. Badesch has received grant monies from the National
Institutes of Health. He has received grant monies from GlaxoSmithKline, United Therapeutics/LungRx, Actelion, Lilly/ICOS,
Encysive, Pfizer, Myogen/Gilead, and CoTherix. He has received
consultant fees from GlaxoSmithKline, Actelion, Myogen/Gilead,
CoTherix, Pfizer, United Therapeutics, Mondo-Biotech, Biogen
IDEC, PR Pharmaceuticals, Forrests Labs, Scios, Amgen, Biovale Pharmaceuticals/Clarus Health, and Johnson & Johnson. He
has served on the speaker’s bureau for GlaxoSmithKline, Actelion, Myogen/Gilead, Encysive, CoTherix, Pfizer, United Therapeutics, Mondo-Biotech, and Biogen IDEC. He has served on
the board of directors for the Pulmonary Hypertension Association and the American Thoracic Society.
Dr. Abman has served as a scientific advisor for INO Therapeutics.
Dr. Simonneau has received grant monies from, served on the
speaker’s bureau for, and served on the advisory committees for
Actelion, Pfizer, Schering, United Therapeutics, and GlaxoSmithKline.
Dr. Rubin has received university grant monies from the National
Heart, Lung, and Blood Institute. He has received grant monies
from Actelion, Pfizer, United Therapeutics, Mondo-Biotech, MD
Primer, and Gilead. He is a shareholder in LungRx. He has
received consultant fees from the National Heart, Lung, and
Blood Institute; Actelion; Pfizer; United Therapeutics; ProQuest;
Bayer Schering; and Mondo-Biotech. He is on the advisory
committees for Actelion, Pfizer, LungRx, MD Primer, and
Encysive.
Dr. McLaughlin has received grant monies from Actelion, Encysive, LungRx, Pfizer, and United Technologies. She has served
on the speaker’s bureau and advisory committees for Actelion,
Gilead, and Pfizer.
Manuscript received November 1, 2006; revision accepted February 9, 2007.
Reproduction of this article is prohibited without written permission
from the American College of Chest Physicians (www.chestjournal.
org/misc/reprints.shtml).
Correspondence to: David B. Badesch, MD, FCCP, University of
Colorado Health Sciences Center, Box C-272, 4200 E. Ninth Ave,
Denver, CO 80262; e-mail: David.Badesch@UCHSC.edu
DOI: 10.1378/chest.06-2674
1918
mittee of the ACCP authorized an update of the
medical treatment guidelines.1 Lewis Rubin, MD,
FCCP, was again selected to chair the panel. A small
subset of authors from the original guideline were
requested to participate in the update. In October
2005, the group met in Montreal to plan the revision
and to cultivate consensus on the approach to the
new treatment algorithm.
The authors performed computerized searches of
the literature for studies on the medical treatment of
PAH that were published prior to September 1,
2006. Only English-language articles were included.
We selected studies of therapeutic agents in the
following classes: prostanoids, endothelin receptor
antagonists, and phophodiesterase inhibitors. As in
the previous guidelines,1 we considered studies conducted among patients with known or suspected
idiopathic PAH (IPAH) or PAH occurring in association with underlying collagen vascular disease, and
congenital heart disease. Also in a manner consistent
with the previous statement, we excluded studies of
pulmonary hypertension (PH) associated with
COPD or other parenchymal lung disease, highaltitude PH, or cardiac disease (eg, left-heart failure,
valvular heart disease) except congenital heart disease. This article provides an update to the previously published guidelines based on this current
body of literature. The original guidelines have been
summarized, a discussion of new studies has been
added, and the treatment algorithm has been revised
to take into account recent developments in therapy.
The recommendations in this guideline, like those in
the 2004 edition, are based on the same grading
system (Table 2), in which the strength of the
recommendation results from the interaction of two
components: the quality of the evidence, and the net
benefit of the therapy to the patient4 (Table 3).
This update provides evidence-based treatment
recommendations for physicians involved in the
care of patients with PAH. No financial support
was provided by any pharmaceutical companies for
the development of this update. Any conflicts of
interest were required to be disclosed by all
authors and included in this document. This
guideline was reviewed and approved by the Pulmonary Vascular NetWork, Health and Science
Policy Committee, and ultimately by the Board of
Regents of the ACCP.
Calcium-Channel Antagonists
A small number of patients with IPAH, who
demonstrate a favorable response to acute vasodilator testing at the time of cardiac catheterization,
will do well with calcium-channel blocker (CCB)
Table 1—Summary of Recommendations From the First Edition of this Guideline*
Guideline No.
Screening, early detection, and
diagnosis of PAH
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
Recommendations
Genetic testing and professional genetic counseling should be offered to relatives of
patients with familial PAH.
Patients with IPAH should be advised about the availability of genetic testing and
counseling for their relatives.
In patients with a suspicion of PAH, ECG should be performed to screen for a
spectrum of cardiac anatomic and arrhythmic problems. ECG lacks sufficient
sensitivity to serve as an effective screening tool for PAH but contributes prognostic
information in patients with known PAH.
In patients with a suspicion of PAH, chest radiography should be performed to reveal
features supportive of a diagnosis of PAH and to lead to diagnoses of underlying
diseases.
In patients with a clinical suspicion of PAH, Doppler echocardiography should be
performed as a noninvasive screening test that can detect PH, although it may be
imprecise in determining actual pressures compared to invasive evaluation in a
portion of patients.
In patients with a clinical suspicion of PAH, Doppler echocardiography should be
performed to evaluate the level of right ventricular systolic pressure and to assess the
presence of associated anatomic abnormalities such as right atrial enlargement, right
ventricular enlargement, and pericardial effusion.
In asymptomatic patients at high risk, Doppler echocardiography should be performed
to detect elevated pulmonary arterial pressure.
In patients with suspected or documented PH, Doppler echocardiography should be
obtained to look for left ventricular systolic and diastolic dysfunction, left-sided
chamber enlargement, or valvular heart disease.
In patients with suspected or documented PH, Doppler echocardiography with contrast
should be obtained to look for evidence of intracardiac shunting.
In patients with unexplained PAH, testing for connective tissue disease and HIV
infection should be performed.
In patients with PAH, ventilation-perfusion scanning should be performed to rule out
CTEPH; a normal scan effectively excludes a diagnosis of CTEPH.
In patients with PAH, contrast-enhanced chest CT or MRI should not be used to
exclude the diagnosis of CTEPH.
In patients with PAH and a ventilation/perfusion scan suggestive of CTEPH, pulmonary
angiography is required for accurate diagnosis and best anatomic definition to assess
operability.
In patients with PAH, testing of pulmonary function and arterial blood oxygenation
should be performed to evaluate for the presence of lung disease.
In patients with systemic sclerosis, pulmonary function testing with Dlco should be
performed periodically (every 6 to 12 mo) to improve detection of pulmonary vascular
or interstitial disease.
In patients with PAH, lung biopsy is not routinely recommended because of the risk,
except under circumstances in which a specific question can only be answered by
tissue examination.
In patients with suspected PH, right-heart catheterization is required to confirm the
presence of PH, establish the specific diagnosis, and determine the severity of PH.
In patients with suspected PH, right-heart catheterization is required to guide therapy.
In patients with PAH, serial determinations of functional class and exercise capacity
assessed by the 6MW test provide benchmarks for disease severity, response to
therapy, and progression.
Medical therapy for PAH
1
2
3
4
5
6
7
8
9
16
a
b
17
Patients with IPAH should undergo acute vasoreactivity testing using a short-acting
agent such as IV epoprostenol, adenosine, or inhaled nitric oxide.
Patients with PAH associated with underlying processes, such as scleroderma or
congenital heart disease, should undergo acute vasoreactivity testing.
Patients with PAH should undergo vasoreactivity testing by a physician experienced in
the management of pulmonary vascular disease.
Patients with IPAH, in the absence of right-heart failure, demonstrating a favorable
acute response to vasodilator (defined as a fall in PAPm of at least 10 mm Hg to ⱕ 40
mm Hg, with an increased or unchanged cardiac output), should be considered
candidates for a trial therapy with an oral calcium-channel antagonist.
Patients with PAH associated with underlying processes such as scleroderma or
congenital heart disease, in the absence of right-heart failure, demonstrating a
favorable acute response to vasodilator (defined as a fall in pulmonary artery pressure
of at least 10 mm Hg to ⱕ 40 mm Hg, with an increased or unchanged cardiac
output), should be considered candidates for a trial of therapy with an oral calciumchannel antagonist.
In patients with PAH, CCBs should not be used empirically to treat PH in the absence
of demonstrated acute vasoreactivity.
Patients with IPAH should receive anticoagulation with warfarin.
In patients with PAH occurring in association with other underlying processes, such as
scleroderma or congenital heart disease, anticoagulation should be considered.
In patients with PAH, supplemental oxygen should be used as necessary to maintain
oxygen saturations at ⬎ 90% at all times.
Children with PAH:
With right-heart failure or with hypercoagulable state, administer anticoagulation with
warfarin.
Without right-heart failure or with hypercoagulable state, administer anticoagulation with
warfarin; for children ⬍ 5 years of age, lower target international normalized ratios are
recommended.
In patients with PAH, pregnancy should be avoided, or termination recommended.
Grading†
Level of evidence: expert opinion; benefit: intermediate; grade of
recommendation: E/A
recommendation: E/A
Quality of evidence: low; benefit: small/weak; strength of
recommendation: C
Quality of evidence: low; benefit: intermediate; strength of
recommendation: C
Quality of evidence: fair; benefit: substantial; strength of
recommendation: A
Quality of evidence: expert opinion, benefit: intermediate; strength of
recommendation: E/B
Quality of evidence: expert opinion; benefit: intermediate; strength of
recommendation: E/B
Quality of evidence: good; benefit: substantial; strength of
recommendation: A
Quality of evidence: fair; benefit: intermediate; strength of
recommendation: B
Quality of evidence: expert opinion; benefit: intermediate; strength of
recommendation: E/A
Quality of evidence: low; benefit: substantial; strength of
recommendation: B
Quality of evidence: low; benefit: negative; strength of recommendation:
D
Quality of evidence: expert opinion; benefit: substantial; strength of
recommendation: E/A
recommendation: B
Quality of evidence: fair; benefit: intermediate; strength of
recommendation: B
Quality of evidence: expert opinion; benefit: substantial; strength of
recommendation: E/A
Quality of evidence: good; benefit: substantial; strength of
recommendation: A
recommendation: B
Quality of evidence: good; benefit: intermediate; strength of
recommendation: A
Level of evidence: fair; benefit: substantial; grade of recommendation: A
Level of evidence: expert opinion; benefit: small/weak; grade of
recommendation: E/C
Level of evidence: expert opinion; benefit: substantial; grade of
recommendation: E/A
Level of evidence: low; benefit: substantial; grade of recommendation: B
recommendation: E/B
recommendation: E/A
Level of evidence: fair; benefit: intermediate; grade of recommendation:
B
Level of evidence: expert opinion; benefit: small/weak; grade of
recommendation: E/C
recommendation: E/A.
Level of evidence: expert opinion; net benefit: intermediate; strength of
recommendation: E/B
Level of evidence: expert opinion; net benefit: small/weak; strength of
recommendation: E/C
Level of evidence: good; benefit: substantial; grade of recommendation:
A
CHEST / 131 / 6 / JUNE, 2007
1919
Table 1—Continued
Guideline No.
Surgical treatments/interventions for
PAH
1
2
3
4
5
6
7
8
9
10
11
PAH and sleep-disordered breathing
1
2
3
4
Prognosis of PAH
1
Recommendations
Grading†
In select patients with PAH unresponsive to medical management, atrial septostomy
should be considered.
In patients with PAH, atrial septostomy should be performed only at institutions with
significant procedural and clinical experience.
Patients with suspected CTEPH should be referred to centers experienced in the
procedure for consideration of pulmonary thromboendarterectomy.
In patients with operable CTEPH, pulmonary thromboendarterectomy is the treatment
of choice for improved hemodynamics, functional status, and survival.
In patients with CTEPH deemed inoperable or with significant residual postoperative
PH, balloon dilation, PAH medical therapy, or lung transplantation may be
considered.
PAH patients with NYHA functional class III and IV symptoms should be referred to a
transplant center for evaluation and listing for lung or heart-lung transplantation
Listed patients with PAH whose prognosis remains poor despite medical therapy should
undergo lung or heart-lung transplantation
In patients with PAH who are undergoing transplantation, the procedure of choice is a
bilateral lung transplant.
In children with PAH who are undergoing transplantation, the procedure of choice is a
bilateral lung transplant.
In adult patients with PAH and simple congenital heart lesions, bilateral lung transplant
with repair of the cardiac defect is the procedure of choice.
In adult patients with PAH and complex congenital heart disease who are undergoing
transplant, HLT is the procedure of choice.
Quality of evidence: low; net benefit: intermediate; strength of
recommendation: C
Quality of evidence: expert opinion; net benefit: substantial; strength of
recommendation: E/A
recommendation: E/A
In the evaluation of patients with PAH, an assessment of sleep-disordered breathing is
recommended.
In the evaluation of a patient with PAH for sleep-disordered breathing,
polysomnography is recommended if OSA is suspected as the etiology, if a screening
test for OSA is positive, or if a high clinical suspicion for OSA is present.
In the management of patients with OSA, routine evaluation for the presence of PAH is
not recommended.
In patients with OSA and PAH, treatment of OSA with positive airway pressure therapy
should be provided with the expectation that pulmonary pressures will decrease,
although they may not normalize, particularly when PAH is more severe.
Quality of evidence: low; net benefit: small/weak; strength of
recommendation: C
Quality of evidence: expert opinion; net benefit: intermediate; strength of
recommendation: E/B
Advance NYHA functional class.
Quality of evidence: good; net benefit: substantial; strength of
recommendation: A
recommendation: A
recommendation: A
Quality of evidence: fair; net benefit: substantial; strength of
recommendation: A
recommendation: A
Quality of evidence: fair; net benefit: intermediate; strength of
recommendation: B
recommendation: C
recommendation: C
recommendation: C
recommendation: C
recommendation: A
2
Low 6MW distance.
3
Presence of a pericardial effusion.
4
Elevated mean right atrial pressure.
5
Reduced cardiac index.
6
Elevated PAPm.
7
Elevated Doppler right ventricular ([tei]) index.
8
Low V˙o2max and low peak exercise systolic and diastolic BP as determined by
cardiopulmonary exercise testing.
ECG findings of increased P wave amplitude in lead II, qR pattern in lead V1, and
World Health Organization criteria for right ventricular hypertrophy.
Elevated brain natriuretic peptide (⬎ 180 pg/mL).
9
10
11
12
13
In patients with IPAH treated with epoprostenol, persistence of NYHA functional class
III or IV status after at least 3 mo of therapy may be used to predict a worse
prognosis.
In patients with scleroderma associated PAH, reduced Dlco (⬍ 45% of predicted) may
be used to predict a worse prognosis.
In pediatric IPAH patients, younger age at diagnosis may be used to predict a worse
prognosis.
Level of evidence: low; benefit: small/weak; grade of recommendation: C
Level of evidence: low; benefit: substantial: grade of recommendation: B
Level of evidence: fair; benefit: substantial: grade of recommendation: A
Level of evidence: low; benefit: Intermediate; grade of recommendation:
C
Level of evidence: low; benefit: intermediate; grade of recommendation:
C
Level of evidence: low; benefit: Substantial; grade of recommendation: B
Quality of evidence: low; net benefit: none; strength of recommendation:
I
recommendation: C
recommendation: C
recommendation: C
*CTEPH ⫽ chronic thromboembolic PH; Dlco ⫽ diffusion capacity of the lung for carbon monoxide; HLT ⫽ heart-lung transplant;
OSA ⫽ obstructive sleep apnea; V˙o2max ⫽ maximum oxygen uptake.
†Recommendation designations are defined in Table 2.
therapy. Since publication of the original ACCP
guidelines, an important article10 has further clarified the role of CCBs in the IPAH population.
Sitbon and colleagues10 reported results of a retrospective analysis of 557 IPAH patients tested
acutely with IV epoprostenol or inhaled nitric
oxide. Using a criteria of a ⬎ 20% decrease in both
PAPm and pulmonary vascular resistance (PVR),
1920
only 70 patients (12.6%) displayed vasoreactivity.
Long-term CCB responders were defined as patients in New York Heart Association (NYHA)
functional class I or II with a sustained hemodynamic improvement after at least 1 year without
the addition of other PAH-specific therapy. Of the
70 patients who displayed acute vasoreactivity,
only 38 patients (6.8% of the overall study group)
Table 2—Quality of Evidence, Net Benefit, and Strength of Recommendation
Variables
Description
Quality of the evidence
Good
Fair
Low
Expert opinion
Evidence is based on good randomized controlled trials or metaanalyses.
Evidence is based on other controlled trials or RCTs with minor flaws.
Evidence is based on nonrandomized, case-control, or other observational studies.
Evidence is based the consensus of the carefully selected panel of experts in the topic field.
There are no studies that meet the criteria for inclusion in the literature review.
Net benefit
Substantial
Intermediate
Small/weak
None
Conflicting
Negative
Strength of recommendation
A
B
C
D
I
E/A
E/B
E/C
E/D
Strong recommendation
Moderate recommendation
Weak recommendation
Negative recommendation
No recommendation possible (inconclusive)
Strong recommendation based on expert opinion only
Moderate recommendation based on expert opinion only
Weak recommendation based on expert opinion only
Negative recommendation based on expert opinion only
had a favorable long-term clinical response to
long-term CCB therapy. These patients exhibited
a more pronounced reduction in PAPm, reaching
an absolute PAPm of 33 ⫾ 8 mm Hg (⫾ SD) with
acute vasodilator testing. As a result, the consensus definition of a favorable response is now
defined as a fall in PAPm ⱖ 10 mm Hg, to a PAPm
ⱕ 40 mm Hg, with an unchanged or increased
cardiac output. Patients with IPAH who meet
these criteria may be treated with CCBs. True
responders to vasodilators (CCBs) are very uncommon among patients with other forms of PAH
(non-IPAH, or PAH occurring in association with
underlying disease processes). Long-acting nifedipine or diltiazem, or amlodipine are suggested.
Due to its potential negative inotropic effects,
verapamil should be avoided. Patients should be
followed up closely for both safety and efficacy,
with an initial reassessment after 3 months of
therapy.10 If a patient does not improve to func-
tional class I or II, additional or alternative PAH
therapy should be instituted.
Prostanoids
Epoprostenol
In a 12-week, prospective, multicenter, randomized,
controlled, open-label trial,11 continuously IV infused
epoprostenol plus conventional therapy (including oral
vasodilators [CCBs], anticoagulation, diuretic, digoxin, and
oxygen) was compared to conventional therapy alone in 81
patients with severe IPAH (NYHA class III or IV).
Exercise capacity improved in the 41 patients treated with
epoprostenol (median 6 min walk [6MW] distance, 362 m
at 12 weeks, vs 315 m at baseline), and decreased in the 40
patients treated with conventional therapy alone (204 m at
12 weeks vs 270 m at baseline; p ⬍ 0.002 for the comparison of the treatment groups). There were also improvements in indexes of the quality of life, hemodynamics, and
Table 3—Relationship of Strength of the Recommendations Scale to Quality of Evidence and Net Benefits*
Net Benefit
Quality of Evidence
Good
Fair
Low
Expert opinion
Substantial
Intermediate
Small/Weak
None
Conflicting
Negative
A
A
B
E/A
A
B
C
E/B
B
C
C
E/C
D
D
I
I
I
I
I
I
D
D
D
E/D
*See Table 2 for definition of designations.
CHEST / 131 / 6 / JUNE, 2007
1921
survival. A multicenter, randomized, controlled, openlabel study12 of long-term IV epoprostenol treatment in
patients with PAH occurring in association with the
scleroderma spectrum of disease showed improvement in
exercise capacity and hemodynamics. Exercise capacity
improved with epoprostenol (median 6MW distance,
316 m at 12 weeks, compared with 270 m at baseline) but
decreased with conventional therapy (192 m at 12 weeks,
compared with 240 m at baseline). The difference between treatment groups in the median distance walked at
week 12 was 108 m (95% confidence interval CI, 55.2 m
to 180.0 m) [p ⬍ 0.001]. Hemodynamics also improved,
however a survival advantage was not demonstrated. Two
large long term observation series have documented an
improvement in survival in patients with IPAH treated
with epoprostenol compared to either historical control
subjects or predicted survival based on the National
Institutes of Health Registry equation.13,14
Treprostinil
A placebo-controlled trial of subcutaneously infused treprostinil in patients with functional class II,
III, or IV PAH (IPAH or PAH associated with
connective tissue disease or congenital systemic to
pulmonary shunts) demonstrated improved exercise
capacity as measured by the 6-min walk (6MW)
distance (median between treatment group difference 16 m (p ⫽ 0.006).15 This effect appeared to be
dose related, and subcutaneous dosing may be limited by infusion site pain and reaction. Given potential advantages over IV epoprostenol, including a
longer half-life, IV treprostinil has been studied
recently. In an open-label study, Tapson et al16
treated 16 functional class III or IV PAH patients
with IV treprostinil. After 12 weeks of therapy, 6MW
distance improved by a mean of 82 m, from
319 ⫾ 22 to 400 ⫾ 26 m (p ⫽ 0.001) [⫾ SE]. There
were also improvements in hemodynamics including
PAPm (⫺ 4.2 mm Hg, p ⫽ 0.03), cardiac index
(⫹ 0.47 L/min/m2, p ⫽ 0.002), and PVR index
(⫺ 9.4 U/m2, p ⫽ 0.001) at week 12 compared to
baseline. One death, which was thought not to be
related to the study drug, occurred during the
12-week study in a patient who received 3 days of IV
treprostinil and died 2 weeks later. In a similar
open-label trial, Gomberg-Maitland et al17 transitioned 31 functional class II and III PAH patients
from IV epoprostenol to IV treprostinil. Twentyseven patients completed the 12-week study, and 4
patients were transitioned back to epoprostenol.
Exercise endurance as measured by the 6MW distance was maintained among the patients completing
the transition (438 ⫾ 16 m at baseline, 439 ⫾ 16 m
at week 12) [⫾ SD]. At week 12, there was a modest
increase in PAPm of 4 ⫾ 1 mm Hg (p ⬍ 0.01) and
1922
reduction in cardiac index of 0.4 ⫾ 0.1 L/min/m2
(p ⫽ 0.01). Notably, the dose of IV treprostinil at the
end of 12 weeks was more than twice the dose of IV
epoprostenol at the start of the study: 83 ng/kg/min
vs 40 ng/kg/min. In 2004, the US Food and Drug
Administration (FDA) approved the use of IV
treprostinil in NYHA functional class II, III, and IV
PAH patients in whom subcutaneous infusion is not
tolerated.
Iloprost
A 3-month, randomized, double-blind, placebocontrolled, multicenter trial of iloprost via inhalation
six to nine times per day utilized a composite primary
end point of a 10% improvement in the 6MW
distance and NYHA functional class improvement in
the absence of clinical deterioration or death.18 This
composite end point was achieved in 17% of treated
patients compared to 5% in patients receiving placebo (p ⫽ 0.007). The treatment effect on the 6MW
distance was a mean increase of 36 m in the overall
population in favor of iloprost (p ⫽ 0.004) and 59 m
in the subgroup of patients with IPAH. Longer-term
data regarding inhaled iloprost are conflicting. In a
1-year, open, uncontrolled study19 of 24 patients
with IPAH, aerosolized iloprost at a daily dose of 100
to 150 ␮g, six to eight inhalations per day improved
exercise capacity (mean increase in 6MW distance,
75 m) and pulmonary hemodynamics. More recently, Opitz et al20 prospectively followed up 76
NHYA functional class II or III IPAH patients
treated with inhaled iloprost. During the follow-up
period of 535 ⫾ 61 days, 11 patients (14%) died, 6
patients (9%) underwent transplantation, 25 patients
(33%) were switched to IV prostanoids, 16 patients
(23%) received additional/oral PAH therapies, and
12 patients (17%) discontinued inhaled iloprost for
other reasons. Event-free survival rates at 1 year and
2 years were 53% and 29%, respectively.
Most recently, inhaled iloprost has been studied in
patients who remain symptomatic (NYHA functional
class III or IV) while receiving a stable dose of
bosentan for at least 3 months.21 In this multicenter,
placebo-controlled, randomized trial, 67 patients
with PAH (94% NYHA functional class III; mean
baseline 6MW, 355 m) were randomized to receive
inhaled iloprost, (5 ␮g; six to nine times per day) or
placebo. After 12 weeks, the primary efficacy measure, postinhalation 6-min walk distance, improved
by 30 m in the iloprost group and 4 m in the placebo
group, for a placebo-adjusted difference of ⫹ 26 m
(p ⫽ 0.051). There were also improvements in
NYHA functional class (p ⫽ 0.002), time to clinical
worsening (p ⫽ 0.022), and postinhalation PAPm
(p ⬍ 0.001) and PVR p ⬍ 0.001). Combination therClinical Practice Guidelines
apy appeared to be safe and well tolerated. Inhaled
iloprost was approved by the FDA in 2004 for
functional class III and IV PAH, and in 2005 a brief
summary of the results of the add-on study was
included in the package insert.
Endothelin Antagonists
Bosentan
The first randomized, double-blind, placebo-controlled, multicenter study22 of bosentan demonstrated an improvement in the 6MW distance of
70 m (from 360 ⫾ 19 m at baseline to 430 ⫾ 14 m at
week 12; p ⬍ 0.05), whereas no improvement was
seen with placebo (355 ⫾ 25 m at baseline and
349 ⫾ 44 m at week 12). Treatment with bosentan
also improved cardiopulmonary hemodynamics and
functional class. Asymptomatic increases in hepatic
aminotransferases were observed in two bosentantreated patients. In a second double-blind, placebocontrolled study (the Bosentan Randomized Trial of
Endothelin Antagonist Therapy for Pulmonary Hypertension-1 Study23), bosentan (125 or 250 mg bid)
was evaluated in 213 patients with functional class
III and IV PAH (either primary or associated with
connective tissue disease), for a minimum of 16
weeks (62.5 mg bid for 4 weeks then target dose).
Bosentan improved the 6MW distance by 36 m,
whereas deterioration (– 8 m) was seen with placebo.
The difference between treatment groups in the
mean change in 6MW distance was 44 m in favor of
bosentan (95% confidence interval, 21 to 67 m;
p ⫽ 0.0002). The risk of clinical worsening was
reduced by bosentan compared to placebo
(p ⫽ 0.0015, log-rank test). Abnormal hepatic function test findings, syncope, and flushing occurred
more frequently in the bosentan group.
Two important articles describing longer-term
outcomes with bosentan therapy have been recently
published. In the first, McLaughlin et al24 found that
first-line therapy with bosentan, with the subsequent
addition or transition to other therapy as necessary,
resulted in Kaplan-Meier survival estimates of 96%
at 12 months and 89% at 24 months. In contrast,
predicted survival rates from the National Institutes
of Health Registry formula are 69% and 57%, respectively. In addition, at the end of 12 months and
24 months, 85% and 70% of patients, respectively,
remained alive and receiving bosentan monotherapy.
Factors that predicted a worse outcome included
World Health Organization functional class IV and
6MW distance below the median (358 m) at baseline. In the second study, Sitbon et al25 compared
survival in patients with functional class III IPAH
treated with bosentan with historical data from simwww.chestjournal.org
ilar patients treated with epoprostenol. Baseline
factors for the 139 patients treated with bosentan
and the 346 patients treated with epoprostenol suggested that the epoprostenol cohort had more severe
disease. Kaplan-Meier survival estimates after 1 year
and 2 years were 97% and 91%, respectively, in the
bosentan cohort, and 91% and 84% in the epoprostenol cohort. Cox regression analyses adjusting for
differences in baseline factors showed a greater
probability of death in the epoprostenol cohort.
When matched cohorts of 83 patients each were
selected, survival estimates were similar. In the
bosentan cohort, 87% and 75% of patients followed
up for 1 year and 2 years, respectively, remained on
monotherapy. No evidence was found to suggest that
initial treatment with oral bosentan, followed by or
with the addition of other treatment if needed,
adversely affected the long-term outcome compared
with initial IV epoprostenol in patients with class III
IPAH.
Bosentan has also been studied in children with
IPAH and PAH associated with congenital heart
disease or connective tissue disease.26 In this
retrospective study,26 86 children started bosentan
with or without concomitant IV epoprostenol or
subcutaneous treprostinil therapy. At the cutoff
date, 68 patients (79%) were still treated with
bosentan, 13 patients (15%) had treatment discontinued, and 5 patients (6%) had died. Median
exposure to bosentan was 14 months. In 90% of
the patients (n ⫽ 78), functional class improved
(46%) or was unchanged (44%) with bosentan
treatment. PAPm and PVR decreased (64 ⫾ 3 to
57 ⫾ 3 mm Hg, p ⫽ 0.005; and 20 ⫾ 2 to 15 ⫾ 2
U/m2, p ⫽ 0.01, respectively; n ⫽ 49 [⫾ SEM]).
Kaplan-Meier survival estimates at 1 year and 2
years were 98% and 91%, respectively.
Most recently, Galie et al27 reported the results of
a multicenter, double-blind, randomized, and placebo-controlled study of bosentan therapy in patients
with functional class III Eisenmenger syndrome
(Bosentan Randomized Trial of Endothelin Antagonist Therapy for Pulmonary Hypertension-5). Fiftyfour patients were randomized 2:1 to bosentan
(n ⫽ 37) or placebo (n ⫽ 17) for 16 weeks. The
placebo-corrected effect on systemic pulse oximetry
was 1.0% (95% confidence interval, ⫺ 0.7 to 2.8),
demonstrating that bosentan did not worsen oxygen
saturation. Compared with placebo, bosentan reduced
PVR
index
(⫺ 472.0
dyne䡠s䡠cm⫺5;
p ⫽ 0.0383). PAPm decreased (⫺ 5.5 mm Hg;
p ⫽ 0.0363), and exercise capacity increased (53.1
m; p ⫽ 0.0079). Treatment was discontinued in four
patients as a result of adverse events: two patients
(5%) in the bosentan group, and two patients (12%)
in the placebo group. Bosentan is currently approved
CHEST / 131 / 6 / JUNE, 2007
1923
by the FDA for the treatment of patients with
functional class III-IV PAH.
Sitaxsentan
In the first randomized, double-blind, placebocontrolled trial28 with sitaxsentan (an endothelin A
receptor selective antagonist) in PAH (the Sitaxsentan to Relieve Impaired Exercise-1 study), 178
NYHA functional class II, III and IV patients with
either IPAH, PAH related to connective tissue disease, or PAH related to congenital systemic to
pulmonary shunts, sitaxsentan improved exercise capacity (6MW distance) and functional class after 12
weeks of treatment. The treatment effects in the
sitaxsentan groups were 35 m (p ⬍ 0.01) for the
100-mg dose and 33 m (p ⬍ 0.01) for the 300-mg
dose. NYHA functional class and cardiopulmonary
hemodynamics also improved. The incidence of liver
function abnormalities was more favorable for the
100-mg dose. The most frequently reported clinical
adverse events with sitaxsentan treatment were
headache, peripheral edema, nausea, nasal congestion, and dizziness, and the most frequently reported
laboratory adverse event was increased international
normalized ratio or prothrombin time related to the
effect of sitaxsentan on inhibition of CYP2C9 P450
enzyme, the principal hepatic enzyme involved in
the metabolism of warfarin.
A second double-blind, placebo-controlled trial
with sitaxsentan in PAH (the Sitaxsentan to Relieve
Impaired Exercise-2 study29) randomized 247 PAH
patients (245 were treated) with IPAH, or PAH
associated with connective tissue disease or congenital heart disease: placebo (n ⫽ 62); sitaxsentan, 50
mg (n ⫽ 62) or 100 mg (n ⫽ 61); or open-label
bosentan (6MW tests, Borg dyspnea scores, and
functional class assessments third-party blind;
n ⫽ 60). The primary end point was change in 6MW
distance from baseline to end of study. At week 18,
patients treated with sitaxsentan, 100 mg, had an
increased 6MW distance compared with the placebo
group (31.4 m, p ⫽ 0.03), and an improved functional class (p ⫽ 0.04). The placebo-subtracted treatment effect for sitaxsentan, 50 mg, was 24.2 m
(p ⫽ 0.07), and for open-label bosentan was 29.5 m
(p ⫽ 0.05). The incidence of elevated hepatic
transaminases (more than three times the upper
limit of normal) was 6% for placebo; 5% for sitaxsentan, 50 mg; 3% for sitaxsentan, 100 mg; and 11%
for bosentan. A new drug application is pending with
the FDA.
Ambrisentan
An initial, phase two study30 examined the efficacy
and safety of four doses of ambrisentan, an oral
1924
endothelin type A receptor-selective antagonist, in
patients with PAH. In this double-blind, dose-ranging study,30 64 patients with functional class II and
III IPAH or PAH associated with connective tissue
disease, anorexigen use, or HIV infection were randomized to receive 1, 2.5, 5, or 10 mg of ambrisentan
qd for 12 weeks followed by 12 weeks of open-label
ambrisentan. At 12 weeks, 6MW distance was increased (⫹ 36.1 m, p ⬍ 0.0001), with similar and
statistically significant increases for each dose group
(range, ⫹ 33.9 to ⫹ 38.1 m). Improvements were
also observed in Borg dyspnea index, functional class,
subject global assessment, PAPm (⫺ 5.2 mm Hg,
p ⬍ 0.0001), and cardiac index (⫹ 0.33 L/min/m2,
p ⬍ 0.0008). Adverse events were mild and unrelated
to dose, including the incidence of elevated serum
aminotransferase concentrations more than three times
the upper limit of normal (3.1%). Two phase III clinical
trials of ambrisentan in patients with PAH have recently been completed, and publication of the results is
pending. Ambrisentan remains an investigational agent
at this time.
Phosphodiesterase Inhibitors
Sildenafil
Sildenafil is a potent and highly specific phosphodiesterase 5 inhibitor that has been previously approved for erectile dysfunction. Several reports31–33
of nonrandomized, single-center studies of PAH
patients treated with long-term sildenafil suggested
promise for sildenafil as a therapeutic agent. A
double-blind, placebo-controlled study (the Sildenafil Use in Pulmonary Arterial Hypertension-1
study,34) randomly assigned 278 patients with symptomatic PAH (either idiopathic or associated with
connective tissue disease or with repaired congenital
systemic-to-pulmonary shunts) to placebo or sildenafil (20, 40, or 80 mg po tid) for 12 weeks. 6MW
distance increased from baseline in all sildenafil
groups; mean placebo-corrected treatment effects
were 45 m (⫹ 13.0%), 46 m (⫹ 13.3%), and 50 m
(⫹ 14.7%) for 20, 40, and 80 mg of sildenafil,
respectively (p ⬍ 0.001 for all comparisons). All sildenafil doses reduced the PAPm, improved the
functional class, and were associated with side effects
such as headache, flushing, epistaxis, dyspepsia, and
diarrhea. The incidence of clinical worsening did not
differ significantly between the patients treated with
sildenafil and those treated with placebo. Among 222
patients completing 1 year of treatment with sildenafil monotherapy, the improvement from baseline
at 1 year in the 6MW was 51 m. It should be noted
that long-term data for sildenafil are available only at
a dose of 80 mg po tid, while the dose approved by
the FDA for the treatment of PAH is 20 mg tid.
Figure 1. Treatment algorithm for PAH. The recommended therapies presented in this algorithm have
been evaluated mainly in those with IPAH, or PAH associated with connective tissue disease or anorexigen
use. Extrapolation to other forms of PAH should be made with caution. Country-specific regulatory agency
approval status and functional class indications for PAH medications vary. (1) Anticoagulation should be
considered for patients with IPAH, and patients with an indwelling catheter for the administration of an IV
prostanoid, in the absence of contraindications. Diuretics and oxygen should be added as necessary. (2) A
positive acute vasodilator response is defined as a fall in PAPm ⱖ 10 mm Hg to ⱕ 40 mm Hg, with an
unchanged or increased cardiac output when challenged with inhaled nitric oxide, IV epoprostenol, or IV
adenosine. (3) Consideration should be given to using a PAH-specific medication such as a phosphodiesterase 5 inhibitor, endothelin receptor antagonist, or prostanoid as first-line treatment instead of a CCB in
patients with PAH that is not IPAH or PAH associated with anorexigen use, or in those in an advanced
functional class (FC) given the exceedingly low long-term response rate to CCB monotherapy in the former
and poor prognosis in the latter. (4) Sustained response to CCB therapy is defined as being in functional
class I or II with normal or near-normal hemodynamics after several months of treatment. (5) The risks and
benefits of treatment in early PAH should be considered. (6) First-line therapy for functional class III
includes bosentan, sildenafil, epoprostenol, inhaled (inh) iloprost, and treprostinil (see text for details). (7)
Most experts recommend IV epoprostenol as first-line treatment for unstable patients in functional class IV.
(8) RCTs studying add-on combination treatment regimens are underway. Designators [A], [B], [C], [D],
and [E/A], [E/C] [E/B] are defined in Table 2. *Not in order of preference. SC ⫽ subcutaneous.
Summary
The paradigm for treatment of PAH continues to
advance rapidly. Multicenter randomized clinical trials
(RCTs) have provided a basis for evidence-based pracwww.chestjournal.org
tice. The treatment algorithm provided (Fig 1) attempts to summarize the current approach to therapy
for PAH. The following brief overview, organized by
functional class, is intended to facilitate clinical application of the algorithm. It should be noted that funcCHEST / 131 / 6 / JUNE, 2007
1925
Table 4 —Summary of Recommendations: Update to the 2004 ACCP Guidelines*
Functional Classes
Functional class II
10
Description
a
PAH patients in functional class II who are not
candidates for, or who have failed, CCB
therapy, may benefit from treatment with:
Sildenafil
b
Subcutaneous treprostinil
c
IV treprostinil
Recommendations
Level of evidence: good; benefit: substantial; grade of
recommendation: A
Level of evidence: low; benefit: small/weak; grade of
recommendation: C. Although treprostinil is FDA
approved for use in patients in functional class II, it
would seldom be recommended in such patients due to
the complexity of administration, side effects, and cost.
Level of evidence: low; benefit: small/weak; grade of
recommendation: C. Although treprostinil is FDA
approved for use in patients in functional class II, it
would seldom be recommended in such patients due to
the complexity of administration, side effects, and cost.
Data pertaining to the treatment of functional class II
patients remain limited, and enrollment in clinical trials is
encouraged.
d
Functional class III
11
b
PAH patients in functional class III who are not
therapy are candidates for long-term therapy
with:
Endothelin receptor antagonists (bosentan), or
sildenafil, in no order of preference
IV epoprostenol
c
Inhaled iloprost
d
e
IV treprostinil
a
Functional class IV
12
recommendation: A
recommendation: A
Level of evidence: good; benefit: intermediate; grade of
recommendation: A
Level of evidence: fair; benefit: intermediate; grade of
recommendation: B
Level of evidence; low; benefit: intermediate; grade of
recommendation: C
a
PAH patients in functional class IV who are not
therapy are candidates for long-term therapy
with IV epoprostenol (treatment of choice).
Other treatments available for the treatment of
functional class IV PAH patients include, in no
hierarchical order:
Endothelin receptor antagonists (bosentan)
b
Inhaled iloprost
c
d
Sildenafil
e
IV treprostinil
13
recommendation: A
recommendation: B
recommendation: B
recommendation: B
Level of evidence: low; benefit: intermediate; grade of
recommendation: C
Level of evidence; low; benefit: intermediate; grade of
recommendation: C
*Refer to Table 1 for recommendations that have not changed since the 2004 guidelines.
tional class is difficult to quantify, and may vary among
patients and care providers. It may not always correlate
with other indexes of disease severity, although it does
correlate with outcome (in patients with IPAH). Accordingly, decisions regarding therapy should take into
1926
account a variety of variables, including but not limited
to functional class. Treating physicians should also
consider cardiopulmonary hemodynamics, 6MW distance, signs and symptoms of right-heart failure, side
effect profile, and drug-drug interactions when making
recommendations to individual patients. Cost may be a
consideration in the choice of therapy.
Functional Class II
Currently, the only therapies approved for functional
class II patients are sildenafil and subcutaneous and IV
treprostinil. Clinical trials with sitaxsentan28,29 and ambrisentan30 included functional class II patients, while an
ongoing trial with bosentan is studying functional class II
patients. Due to the ease of administration and relative
efficacy, sildenafil may be the first choice for most functional class II patients. Enrollment into clinical trials is also
encouraged.
Functional Class III
There are now five drugs in three therapeutic
classes approved by the FDA for the treatment of
patients with functional class III PAH. Rational
therapeutic decisions must be made based on the
evidence outlined above, knowledge of an individual
patient’s specific situation, clinical judgment, and
patient preferences. Most experts now consider one
of the two approved oral therapies (bosentan or
sildenafil, listed in no order of preference) for
patients with “early” functional class III PAH. In
choosing between these agents, clinicians should
consider relative toxicities. For example, patients
with liver abnormalities, or inability to have liver
tests monitored on a monthly basis might be better
served by sildenafil. Patients with ocular disease or
recurrent epistaxis might be better candidates for
bosentan. If cost is a consideration, sildenafil tends to
be less expensive. Patients with more advanced class
III disease may require treatment with a prostanoid,
such as IV epoprostenol or treprostinil, inhaled
iloprost, or subcutaneous treprostinil. It is anticipated that we will soon have evidence regarding the
use of add-on and combination therapy. Until additional evidence becomes available, add-on or combination therapy might be considered in the context of
enrollment into clinical trials.
Functional Class IV
While all currently labeled therapies are approved
for functional class IV patients, based on the quality
of the evidence and the net risk/benefit profile, we
strongly encourage IV epoprostenol as the treatment
of choice for these most critically ill patients. IV
epoprostenol has a rapid and predictable onset of
action, and most experts are familiar with how to
titrate this drug in the acute setting. Experience with
IV treprostinil is accumulating; in some instances
this may be a suitable alternative to IV epoprostenol.
Recognizing that limited data are available on which
to base treatment choices in patients with functional
class IV symptoms, oral, subcutaneous, and inhaled
agents should generally not be used as first-line
therapy in this situation unless the patient refuses IV
therapy or is believed not to be capable of managing
the complex delivery system.
Conclusions
Recommendations regarding therapy obviously
need to be applied in light of the individual patient’s
specific situation (Table 4). The importance of a
thorough diagnostic evaluation, looking for underlying causes and contributing factors, cannot be overemphasized. Educational efforts have contributed to
improved recognition of PAH, facilitating earlier
initiation of therapy. This should contribute to better
clinical outcomes. Due to the complexity of the
diagnostic evaluation required, and the treatment
options available, it continues to be strongly recommended that consideration be given to referral of
patients with PAH to a specialized center. Wellcontrolled clinical trials should continue to lead to
further improvements in the treatment of this very
challenging disease.
References
1 Badesch DB, Abman SH, Ahearn GS, et al. Medical therapy
for pulmonary arterial hypertension: ACCP evidence-based
clinical practice guidelines. Chest 2004; 126:35S– 62S
2 Rubin LJ. Diagnosis and management of pulmonary arterial
hypertension: ACCP evidence-based clinical practice guidelines. Chest 2004; 126:7S–10S
hypertension: ACCP evidence-based clinical practice guidelines. Chest 2004; 126:4S– 6S
4 McCrory DC, Lewis SL. Methodology and grading for pulmonary hypertension evidence review and guideline development. Chest 2004; 126:35S– 62S
5 McGoon M, Gutterman D, Steen V, et al. Screening, early
detection, and diagnosis of pulmonary arterial hypertension:
ACCP evidence-based clinical practice guidelines. Chest
2004; 126:14S–34S
6 Doyle RL, McCrory D, Channick RN, et al. Surgical treatments/interventions for pulmonary arterial hypertension:
ACCP evidence-based clinical practice guidelines. Chest
2004; 126:63S–71S
7 Atwood CW Jr, McCrory D, Garcia JG, et al. Pulmonary
artery hypertension and sleep-disordered breathing: ACCP
evidence-based clinical practice guidelines. Chest 2004; 126:
72S–77S
8 McLaughlin VV, Presberg KW, Doyle RL, et al. Prognosis of
pulmonary arterial hypertension: ACCP evidence-based clinical practice guidelines. Chest 2004; 126:78S–92S
hypertension: ACCP evidence-based clinical practice guidelines. Chest 2004; 126(1 Suppl):45S–92S
10 Sitbon O, Humbert M, Jais X, et al. Long-term response to
calcium channel blockers in idiopathic pulmonary arterial
hypertension. Circulation 2005; 111:3105–3111
11 Barst RJ, Rubin LJ, Long WA, et al. A comparison of
continuous intravenous epoprostenol (prostacyclin) with conCHEST / 131 / 6 / JUNE, 2007
1927
12
13
14
15
16
17
18
19
20
21
22
ventional therapy for primary pulmonary hypertension: the
Primary Pulmonary Hypertension Study Group. N Engl
J Med 1996; 334:296 –302
Badesch DB, Tapson VF, McGoon MD, et al. Continuous
intravenous epoprostenol for pulmonary hypertension due to
the scleroderma spectrum of disease: a randomized, controlled trial. Ann Intern Med 2000; 132:425– 434
Sitbon O, Humbert M, Nunes H, et al. Long-term intravenous epoprostenol infusion in primary pulmonary hypertension: prognostic factors and survival. J Am Coll Cardiol 2002;
40:780 –788
McLaughlin VV, Shillington A, Rich S. Survival in primary
pulmonary hypertension: the impact of epoprostenol therapy.
Circulation 2002; 106:1477–1482
Simonneau G, Barst RJ, Galie N, et al. Continuous subcutaneous infusion of treprostinil, a prostacyclin analogue, in
patients with pulmonary arterial hypertension: a doubleblind, randomized, placebo-controlled trial. Am J Respir Crit
Care Med 2002; 165:800 – 804
Tapson VF, Gomberg-Maitland M, McLaughlin VV, et al.
Safety and efficacy of IV treprostinil for pulmonary arterial
hypertension: a prospective, multicenter, open-label, 12-week
trial. Chest 2006; 129:683– 688
Gomberg-Maitland M, Tapson VF, Benza RL, et al. Transition from intravenous epoprostenol to intravenous treprostinil
in pulmonary hypertension. Am J Respir Crit Care Med 2005;
172:1586 –1589
Olschewski H, Simonneau G, Galie N, et al. Inhaled iloprost
for severe pulmonary hypertension. N Engl J Med 2002;
347:322–329
Hoeper MM, Schwarze M, Ehlerding S, et al. Long-term
treatment of primary pulmonary hypertension with aerosolized iloprost, a prostacyclin analogue. N Engl J Med 2000;
342:1866 –1870
Opitz CF, Wensel R, Winkler J, et al. Clinical efficacy and
survival with first-line inhaled iloprost therapy in patients with
idiopathic pulmonary arterial hypertension. Eur Heart J 2005;
26:1895–1902
McLaughlin VV, Oudiz RJ, Frost A, et al. Randomized study
of adding inhaled iloprost to existing bosentan in pulmonary
arterial hypertension. Am J Respir Crit Care Med 2006;
174:1257–1263
Channick RN, Simonneau G, Sitbon O, et al. Effects of the
1928
23
24
25
26
27
28
29
30
31
32
33
34
dual endothelin-receptor antagonist bosentan in patients with
pulmonary hypertension: a randomised placebo-controlled
study. Lancet 2001; 358:1119 –1123
Rubin LJ, Badesch DB, Barst RJ, et al. Bosentan therapy for
pulmonary arterial hypertension. N Engl J Med 2002; 346:
896 –903
McLaughlin VV, Sitbon O, Badesch DB, et al. Survival with
first-line bosentan in patients with primary pulmonary hypertension. Eur Respir J 2005; 25:244 –249
Sitbon O, McLaughlin VV, Badesch DB, et al. Survival in
patients with class III idiopathic pulmonary arterial hypertension treated with first line oral bosentan compared with an
historical cohort of patients started on intravenous epoprostenol. Thorax 2005; 60:1025–1030
Rosenzweig EB, Ivy DD, Widlitz A, et al. Effects of longterm bosentan in children with pulmonary arterial hypertension. J Am Coll Cardiol 2005; 46:697–704
Galie N, Beghetti M, Gatzoulis MA, et al. Bosentan therapy
in patients with Eisenmenger syndrome: a multicenter, double-blind, randomized, placebo-controlled study. Circulation
2006; 114:48 –54
Barst RJ, Langleben D, Frost A, et al. Sitaxsentan therapy for
pulmonary arterial hypertension. Am J Respir Crit Care Med
2004; 169:441– 447
Barst RJ, Langleben D, Badesch D, et al. Treatment of
pulmonary arterial hypertension with the selective endothelin-A receptor antagonist sitaxsentan. J Am Coll Cardiol 2006;
47:2049 –2056
Galie N, Badesch D, Oudiz R, et al. Ambrisentan therapy for
pulmonary arterial hypertension. J Am Coll Cardiol 2005;
46:529 –535
Ghofrani HA, Wiedemann R, Rose F, et al. Combination
therapy with oral sildenafil and inhaled iloprost for severe
pulmonary hypertension. Ann Intern Med 2002; 136:515–522
Bharani A, Mathew V, Sahu A, et al. The efficacy and
tolerability of sildenafil in patients with moderate-to-severe
pulmonary hypertension. Indian Heart J 2003; 55:55–59
Sastry BK, Narasimhan C, Reddy NK, et al. A study of clinical
efficacy of sildenafil in patients with primary pulmonary
hypertension. Indian Heart J 2002; 54:410 – 414
Galie N, Ghofrani HA, Torbicki A, et al. Sildenafil citrate
therapy for pulmonary arterial hypertension. N Engl J Med
2005; 353:2148 –2157

Medical Therapy for Pulmonary Arterial Hypertension*

Transcription

Similar documents

Project A Registration for Parents 1. Begin at the WCATY homepage

Pulmonary Hypertension in Scleroderma

Puerto Rico: The Face Of PH for the World

Kinetico Yellow Page Program by How the Program Works in Five

Edition 12

Ivana Lulić Jakovljević, Anica Šišović, Gordana Pehnec, Ranka

file

FORMAL TEACHER RECOMMENDATION REQUEST FORM Electronic Submission